Sudden cardiac death in a girl with familiar left-dominant arrhythmogenic cardiomyopathy: a multidisciplinary approach

J Cardiovasc Med (Hagerstown). 2020 May;21(5):391-392. doi: 10.2459/JCM.0000000000000902.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Arrhythmogenic Right Ventricular Dysplasia / complications
  • Arrhythmogenic Right Ventricular Dysplasia / diagnosis
  • Arrhythmogenic Right Ventricular Dysplasia / genetics*
  • Carrier Proteins / genetics*
  • DNA Mutational Analysis
  • Death, Sudden, Cardiac / etiology*
  • Desmoplakins / genetics*
  • Female
  • Genetic Predisposition to Disease
  • Genetic Testing
  • Heredity
  • Humans
  • Myocardium / pathology
  • Pedigree
  • Phenotype

Substances

  • Carrier Proteins
  • DSP protein, human
  • Desmoplakins
  • myosin-binding protein C